Polyol composition for molding flexible polyurethane foam, and flexible polyurethane foam

ABSTRACT

The present invention provides a polyol composition that can secure the stability over time even when a large amount of water is blended in the polyol composition; a flexible polyurethane foam that uses the polyol composition, is low in density and is excellent in durability; and a method for producing the same. The above objects are solved by a polyol composition for molding a flexible polyurethane foam, comprising a polyol component; a catalyst; a foam stabilizer; a foaming agent; and a compatibilizing agent, wherein the compatibilizing agent is an anionic surfactant which has a hydrophilic portion having an alkali metal salt, and which has a hydrophobic portion having an aromatic ring or alternatively a hydrophobic portion not having an aromatic ring but containing 8 or more carbon atoms in total.

TECHNICAL FIELD

The present invention relates to a polyol composition for molding aflexible polyurethane foam, and to a flexible polyurethane foam usingthe composition. More specifically, the present invention relates to alow density flexible polyurethane foam formed from a polyol compositionwhich secures stability over time while a large amount of water of afoaming agent is added thereto, and from polyisocyanate; and a methodfor producing a flexible polyurethane foam.

BACKGROUND ART

Flexible polyurethane foams are widely used in living goods, automotivematerials, clothes, sports and leisure goods, medical materials, civilengineering and construction materials, and the like. Among suchapplication fields, particularly in applications for automobile seatsuch as a seat cushion and a seat back, reduction in density of theflexible polyurethane foam is required, for cost reduction and weightreduction for coping with fuel efficiency regulation.

The flexible polyurethane foam is generally obtained by mixing a polyolcomponent, a catalyst, a foam stabilizer, a foaming agent and apolyisocyanate component, and by reacting the isocyanate group with anactive hydrogen group. In the past, there has been a period whenchlorofluorocarbon type and organic type forming agents were used asfoaming agents, but in recent years, water that reacts with anisocyanate group in polyisocyanate to generate carbonic acid gas hasbecome the mainstream because of environmental concerns. In a flexiblepolyurethane molded foam in which the foam is obtained by foaming andcuring the materials in a mold, such a method is general as to supplytwo liquids of a polyol composition in which a polyol component, acatalyst and a foam stabilizer are previously mixed with water of afoaming agent, and of a polyisocyanate component, to a foamingapparatus, and to mix and discharge the two liquids into the mold via amixing head; and it is effective means for responding to a desire oflowering density to increase the amount of the water to be blended inthe polyol composition and to increase the amount of the carbonic acidgas to be generated.

The polyisocyanate component is roughly divided into a TDI-basedpolyisocyanate component which is mainly consisting of tolylenediisocyanate (TDI), and an MDI-based polyisocyanate component which ismainly consisting of a mixture of diphenylmethane diisocyanate (MDI) andpolyphenyl polymethylene polyisocyanate (P-MDI). As for the TDI-basedpolyisocyanate component, a content of a isocyanate group is high and anamount of carbonic acid gas to be generated per unit weight by areaction with water is large, and accordingly the TDI-basedpolyisocyanate component can lower the density without increasing theamount of the water to be blended so much; but there are such problemsthat the TDI of a raw material tends to easily aggravate a workingenvironment of a production site of the flexible polyurethane foam,because the vapor pressure is high and the toxicity is strong, and thatthe flexible polyurethane foam obtained by TDI which is bifunctionalisocyanate is low in durability.

On the other hand, the MDI-based polyisocyanate component has a tendencyopposite to that of the TDI-based polyisocyanate component, and issuperior to the TDI-based polyisocyanate component in the points of theworking environment and the foam durability, but is low in the contentof the isocyanate group, and needs to blend a large amount of water inorder to lower the density. There has been a problem of aggravating thecompatibility between a hydrophobic component mainly containing apolymer polyol and hydrophilic components such as a catalyst, lowmolecular weight polyol and polyether polyol which contains a largeamount of an ethylene oxide unit, by blending a large amount of water inthe polyol composition, and lowering the stability over time of thepolyol composition. As means for improving the stability over time ofthe polyol composition, it is proposed in Japanese Unexamined PatentPublication No. 2004-002788 to use a polyether polyol which hasoxyethylene units in a specific range and a high primarization ratio ofa terminal end. However, in this method, the compatibility between thehydrophilic component and the hydrophobic component is not sufficientlyimproved for a polyol composition in which such a large amount of wateras to exceed 4.0 mass % is blended. Such a problem tends to occur thatthe polyol composition during storage is decomposed particularly in thesummer season in which ambient temperature is high, and the uniformityof foam performance cannot be kept.

CITATION LIST Patent Literature

Patent Literature 1

Japanese Unexamined Patent Publication No. 2004-002788

SUMMARY OF INVENTION Technical Problem

The present invention has been designed with respect to the abovebackground art, and is directed at providing a polyol composition thatcan secure the stability over time even when a large amount of water isblended in the polyol composition, a flexible polyurethane foam thatuses the polyol composition, is low in density and is excellent indurability; and a method for producing the same.

Solution to Problem

As a result of having made an extensive investigation, the presentinventors have found that the above described problems can be solved bythat a polyol composition contains a specific compatibilizing agent, andhave accomplished the present invention.

Specifically, the present invention includes the following embodiments.

(1) A polyol composition for molding a flexible polyurethane foam,comprising a polyol component (A); a catalyst (B); a foam stabilizer(C); a foaming agent (D); and a compatibilizing agent (E), wherein thecompatibilizing agent (E) is an anionic surfactant having a hydrophilicportion and a hydrophobic portion, and wherein the hydrophilic portionhas a salt consisting of an anionic polar group and an alkali metal, andthe hydrophobic portion has an aromatic ring, or alternatively thehydrophobic portion does not have an aromatic ring but contains 8 ormore carbon atoms in total.

(2) The polyol composition for molding a flexible polyurethane foamaccording to (1), wherein the alkali metal salt of the hydrophilicportion of the compatibilizing agent (E) is a sodium salt.

(3) The polyol composition for molding a flexible polyurethane foamaccording to (1) or (2), wherein the compatibilizing agent (E) is ananionic surfactant having a sodium salt of a naphthalenesulfonic acidformalin condensate.

(4) The polyol composition for molding a flexible polyurethane foamaccording to (1) or (2), wherein the compatibilizing agent (E) is ananionic surfactant having a sodium salt of a dialkyl sulfosuccinate.

(5) The polyol composition for molding a flexible polyurethane foamaccording to (1) or (2), wherein the compatibilizing agent (E) is ananionic surfactant having a sodium salt of an alkylbenzenesulfonic acid.

(6) The polyol composition for molding a flexible polyurethane foamaccording to any one of (1) to (5), wherein the compatibilizing agent(E) is contained in an amount of 0.1 to 5 mass % with respect to thepolyol component (A).

(7) The polyol composition for molding a flexible polyurethane foamaccording to any one of (1) to (6), wherein the polyol component (A)comprises at least one cyclic glycol selected from the group consistingof alicyclic glycols and aromatic glycols.

(8) The polyol composition for molding a flexible polyurethane foamaccording to (7), wherein a content of the at least one cyclic glycolselected from the group consisting of alicyclic glycols and aromaticglycols is 1.5 to 8 mass % with respect to the polyol component (A).

(9) A flexible polyurethane foam comprising: the polyol composition formolding a flexible polyurethane foam according to any one of (1) to (8);and a polyisocyanate component (F).

(10) The flexible polyurethane foam according to (9), wherein thepolyisocyanate component (F) contains diphenylmethane diisocyanate in arange of 50 to 85 mass %, and a total amount of 2,2′-diphenylmethanediisocyanate and 2,4′-diphenylmethane diisocyanate contained in thediphenylmethane diisocyanate is 10 to 50 mass % with respect to a totalamount of the diphenylmethane diisocyanate.

(11) The flexible polyurethane foam according to (9) or (10), wherein anapparent density is less than 40 kg/m³, and a 25% compression hardnessof a foam test piece provided with a skin is 50 to 250 N/314 cm².

(12) The flexible polyurethane foam according to any one of (9) to (11),wherein a coefficient of hysteresis loss is less than 30%, and a wetheat compression strain is less than 20%.

(13) A method for producing a flexible polyurethane foam, comprisingreacting the polyol composition for molding a flexible polyurethane foamaccording to any one of (1) to (8) with a polyisocyanate component (F).

(14) The method for producing a flexible polyurethane foam according to(13), wherein the polyisocyanate component (F) contains diphenylmethanediisocyanate in a range of 50 to 85 mass %, and a total amount of2,2′-diphenylmethane diisocyanate and 2,4′-diphenylmethane diisocyanatecontained in the diphenylmethane diisocyanate is 10 to 50 mass % withrespect to a total amount of the diphenylmethane diisocyanate.

(15) The method for producing a flexible polyurethane foam according to(13) or (14), wherein an apparent density of the flexible polyurethanefoam to be obtained is less than 40 kg/m³, and a 25% compressionhardness of a foam test piece provided with a skin is 50 to 250 N/314cm².

(16) The method for producing a flexible polyurethane foam according toany one of (13) to (15), wherein a coefficient of hysteresis loss of theflexible polyurethane foam to be obtained is less than 30%, and a wetheat compression strain thereof is less than 20%.

Advantageous Effects of Invention

According to the present invention, a flexible polyurethane foam can beobtained which has stability over time of the polyol composition securedand has excellent durability even though the density is low, even in thecase where a large amount of water has been blended in the polyolcomposition, when the flexible polyurethane foam is molded.

DESCRIPTION OF EMBODIMENTS

The present invention will be described in more detail.

The polyol composition for flexible polyurethane foam of the presentinvention comprises a polyol component (A), a catalyst (B), a foamstabilizer (C), a foaming agent (D) and a compatibilizing agent (E),which are described below.

The polyol component (A) is one which forms polyurethane by causingaddition polymerization with diisocyanate, and in the present invention,is preferably at least one selected from the group consisting ofpolyether polyols and polyester polyols. Furthermore, it is morepreferable that a number average molecular weight is 1000 to 10000, andthe number of nominal functional groups is 2 or more. When the numberaverage molecular weight is less than the lower limit, a flexibility ofa foam to be obtained becomes insufficient, and when exceeding the upperlimit, the hardness of the foam tends to decrease. In addition, when thenumber of the nominal functional groups is less than 2, there arises aproblem that a compression residual strain which is an index ofdurability deteriorates. For information, the number of the nominalfunctional groups means the number of theoretical average functionalgroups (number of active hydrogen atoms per molecule), when it isassumed that a side reaction does not occur during the polymerizationreaction of polyol.

Examples of the polyether polyol to be used include polypropyleneethylene polyol and polytetramethylene ether glycol (PTG); and examplesof the polyester polyol to be used include a polyester polyol thatconsists of adipic acid and ethylene glycol, which is a polycondensationtype polyester-based polyol, and polycaprolactone polyol of alactone-based polyester polyol.

As the catalyst (B), various urethanated catalysts known in the relevantfield can be used, and examples thereof include triethylamine,tripropylamine, tributylamine, N-methylmorpholine, N-ethylmorpholine,dimethylbenzylamine, N,N,N′,N′-tetramethylhexamethylenediamine,N,N,N′,N′,N″-pentamethyldiethylenetriamine, bis-(2-dimethylaminoethyl)ether, triethylenediamine,1,8-diaza-bicyclo[5.4.0]undecene-7,1,2-dimethylimidazole,dimethylethanolamine and N,N-dimethyl-N-hexanolamine; further organicacid salts thereof; and also organometallic compounds such as stannousoctoate and zinc naphthenate. In addition, amine catalysts having activehydrogen such as N,N-dimethylethanolamine and N,N-diethylethanolamineare also preferable.

It is preferable that an amount of the catalyst (B) to be added is 0.01to 10 mass % with respect to the polyol component (A). If the amount ofthe catalyst (B) to be added is less than the lower limit value, thecuring tends to be insufficient, and if the amount of the catalyst (B)to be added exceeds the upper limit value, it may occur that themoldability deteriorates.

As the foam stabilizer (C), a usual surfactant is used, and anorganosilicon-based surfactant can be suitably used. Examples of thefoam stabilizer (C) include: SZ-1327, SZ-1325, SZ-1336 and SZ-3601 madeby Dow Corning Toray Co., Ltd.; Y-10366 and L-5309 made by MomentiveCorporation; and B-8724 LF2 and B-8715 LF2 made by Evonik Japan Co.,Ltd.; and F-122 made by Shin-Etsu Chemical Co., Ltd. It is preferablethat an amount of these foam stabilizers is 0.1 to 3 mass % with respectto the polyol component (A).

As the foaming agent (D), water is used. Water reacts with an isocyanategroup to generate carbonic acid gas, and thereby can form foam. Inaddition, an arbitrary foaming agent may be used additionally withwater. For example, a small amount of an organic compound having a lowboiling point such as cyclopentane and isopentane may be concomitantlyused; or it is possible to form foam by using a gas loading device andmixing and dissolving air, nitrogen gas or liquefied carbon dioxide intoa stock solution. An amount of the foaming agent to be added is usually0.5 to 10 mass % with respect to the polyol component (A), but when itis intended to obtain a low density flexible polyurethane foam of whichan apparent density is less than 40 kg/m³, it is preferable to be 4.0 to8.0 mass %, and is further preferable to be 5.0 to 8.0 mass %. If theamount of the foaming agent to be added exceeds the upper limit, thereis the case where foaming resists being stabilized, and if the amount isless than the lower limit, there is the case where the density of thefoam may not be sufficiently lowered. When a large amount of water of4.0 mass % or more is added, it is possible to secure stability overtime of the polyol composition by adding the compatibilizing agent (E)of the present invention.

The compatibilizing agent (E) in the present invention is an anionicsurfactant having a hydrophilic portion and a hydrophobic portion. Thehydrophilic portion of the compatibilizing agent (E) has a salt (alkalimetal salt) consisting of an anionic polar group and an alkali metal;and it is preferable to have an alkali metal salt of sulfonic acid, acarboxylic acid, phosphoric acid or the like, and it is furtherpreferable to have an alkali metal salt of sulfonic acid. Furthermore,it is preferable that the alkali metal salt of the hydrophilic portionis a sodium salt.

In addition, the hydrophobic portion of the compatibilizing agent (E)has an aromatic ring, or alternatively the hydrophobic portion does nothave an aromatic ring but contains 8 or more carbon atoms in total.Here, when the hydrophobic portion has an aromatic ring, it ispreferable that the anionic polar group of the hydrophilic portion isdirectly bonded to the aromatic ring, and the aromatic ring may be apolycyclic aromatic hydrocarbon. In addition, in the case where thecompatibilizing agent (E) has a hydrophobic portion which does not havean aromatic ring but contains contains 8 or more carbon atoms in total,the compatibilizing agent (E) may have such a hydrophobic portion thatthe number of carbon atoms contained, for example, in an alkyl group, analkylene group, an ester group, a carbonate group or the like in thehydrophobic portion is 8 or more in total, and it is preferable that thetotal number is 40 or less. Examples of the anionic surfactant havingthese structures include: an alkali metal salt of a naphthalenesulfonicacid formalin condensate; an alkali metal salt of a dialkylsulfosuccinate; and an alkali metal salt of an alkylbenzenesulfonicacid.

Examples of the alkali metal salt of the naphthalenesulfonic acidformalin condensate include: a sodium salt of a β-naphthalenesulfonicacid formalin condensate; and a sodium salt of an alkylnaphthalenesulfonic acid formalin condensate. Examples of the alkali metal salt ofthe dialkyl sulfosuccinate include: di-2-ethylhexyl sulfosuccinatesodium salt and a sodium salt of di-tridecyl sulfosuccinate. Examples ofthe alkali metal salt of the alkylbenzenesulfonic acid include a sodiumsalt of dodecylbenzenesulfonic acid.

As for the amount of the compatibilizing agent (E) to be added, it ispreferable to contain 0.1 to 5 mass % with respect to the polyolcomponent (A). If the amount is less than the lower limit value, it isdifficult to obtain an effect of improving the compatibility, and if theamount exceeds the upper limit value, the moldability of the foamoccasionally deteriorates.

By using the above described polyol composition comprising the polyolcomponent (A), the catalyst (B), the foam stabilizer (C), the foamingagent (D) and the compatibilizing agent (E), it is possible to secureadequate compatibility even when a large amount of water has beenblended in the polyol composition.

In addition, in the present invention, it is preferable that the polyolcomponent (A) contains at least one cyclic glycol selected from thegroup consisting of alicyclic glycols and aromatic glycols (hereinafterreferred to simply as “cyclic glycol”).

The cyclic glycol is a compound having a cyclic structure in thecompound, and examples of the cyclic glycol include cyclohexane diol,cyclohexane dimethanol, hydroquinone bis(2-hydroxyethyl) ether,dihydroxydiphenyl methane, a hydride of bisphenol A, polyoxyethylenebisphenol ether and polyoxypropylene bisphenol ether. Among these,1,4-cyclohexanedimethanol and polyoxyethylene bisphenol A ether arepreferable, from the viewpoint that an effect of improving the wet heatcompression strain of a flexible polyurethane foam to be obtained ishigh.

It is preferable for the content of the cyclic glycol to be 1.5 to 8mass %, and is more preferable to be 1.5 to 6 mass %, with respect tothe polyol component (A).

In the present invention, the flexible polyurethane foam can be obtainedby mixing the above described polyol composition for molding a flexiblepolyurethane foam and the polyisocyanate component (F), and formingform.

As for the polyisocyanate component (F), it is preferable to usediphenylmethane diisocyanate (hereinafter referred to as MDI) such as4,4′-diphenylmethane diisocyanate (hereinafter referred to as 4,4′-MDI),2,4′-diphenylmethane diisocyanate (hereinafter referred to as 2,4′-MDI)and 2,2′-diphenylmethane diisocyanate (hereinafter referred to as2,2′-MDI), and polyphenylene polymethylene polyisocyanate (hereinafterreferred to as P-MDI), as an isocyanate source. In the presentinvention, various modified products of the above described MDI, amixture of MDI and P-MDI, a urethane modified product, a urea modifiedproduct, an allophanate modified product, a biuret modified product andthe like can also be used.

It is preferable that a rate of MDI content of the polyisocyanatecomponent (F) according to the present invention is in a range of 50 to85 mass %. If the rate of MDI content exceeds 85 mass %, there is apossibility that the storage stability at low temperature of thepolyisocyanate composition to be obtained and the durability of aflexible foam to be obtained are lowered; and on the other hand, if theMDI content is less than 50 mass %, there is a possibility that theelongation of the flexible polyurethane foam decreases and it becomesdifficult to obtain a sufficient foam strength, as the crosslink densityincreases.

Furthermore, it is preferable that the total of a content of 2,2′-MDIand a content of 2,4′-MDI with respect to the total amount of MDI(hereinafter referred to as isomer content) is 10 to 50 mass %.

When the content of 2,2′-MDI and 2,4′-MDI with respect to the totalamount of MDI according to the present invention is less than 10 mass %,there is a possibility that the storage stability at low temperature ofthe obtained polyisocyanate composition is impaired, and there is thecase where it becomes necessary to constantly warm an isocyanate storageplace, pipes and the inside of the foam molding machine. In addition,the molding stability of the flexible polyurethane foam tends to beeasily impaired, and there is the case where foam collapse and the likeoccur in a middle of forming foam. On the other hand, when the contentexceeds 50 mass %, the reactivity is lowered, and there is a possibilitythat such problems occur that a molding cycle is extended, a closed cellratio of foam becomes high, and the foam shrinks after having beenmolded.

In the production of the flexible polyurethane foam of the presentinvention, it is possible to use various well-known additives orauxiliary agents such as fillers like calcium carbonate and bariumsulfate, flame retardants, plasticizers, coloring agents and antifungalagents, as needed.

By use of the polyol composition and the polyisocyanate component asdescribed above in the present invention, it is possible to suitablyobtain such a flexible polyurethane foam that an apparent density isless than 40 kg/m³, and that a 25% compression hardness of a foam testpiece provided with a skin is 50 to 250 N/314 cm², a coefficient ofhysteresis loss thereof is less than 30%, and a wet heat compressionstrain thereof is less than 20%.

In addition, by the polyol component (A) containing the above describedcyclic glycol, the wet heat compression strain is further improved, andthe value can be controlled to less than 15%.

Next, a method for producing the flexible polyurethane foam of thepresent invention will be described.

The flexible polyurethane foam of the present invention can be producedby making a mixture of a polyol component (A), a catalyst (B), a foamstabilizer (C), a foaming agent (D), a compatibilizing agent (E) and apolyisocyanate component (F) react and forming foam.

It is preferable for a molar ratio (NCO/active hydrogen) of the totalisocyanate groups to all the active hydrogen groups in chemicalcompounds containing active hydrogen groups, which include water, in thepolyisocyanate composition of the present invention, at the time ofmixing and foaming, to be 0.7 to 1.4 (isocyanate index (NCO INDEX)=70 to140), and as for an adequate range for the durability and molding cycleof the foam, it is more preferably to be 0.7 to 1.2 (NCO INDEX=70 to120).

When the NCO INDEX is less than 70, the durability lowers and a closedcell property excessively rises; and when the NCO INDEX is higher than120, there is the case where the molding cycle is extended due tounreacted isocyanate which has remained for a long period of time, andcell collapse occurs in a middle of forming foam due to the delay ofchange to high molecular weight.

As for a method for producing the flexible polyurethane foam, it ispossible to use a method for producing a flexible polyurethane moldedfoam (hereinafter referred to as flexible mold foam) of: injecting afoaming stock solution of a mixed liquid of the above described polyolcomponent (A), the catalyst (B), the foam stabilizer (C), the foamingagent (D), the compatibilizing agent (E), and the polyisocyanatecomponent (F) into a mold; and then forming foam and curing the foamingstock solution.

A mold temperature at the time when the above described foaming stocksolution is injected into the mold is usually 30 to 80° C., andpreferably is 45 to 65° C. If the mold temperature at the time when theabove described foaming stock solution is injected into the mold islower than 30° C., the temperature leads to an extension of theproduction cycle due to lowering of the reaction rate: and on the otherhand, if the temperature is higher than 80° C., the reaction betweenwater and isocyanate is excessively promoted, in the reaction of thepolyol and the isocyanate, and there is the case where the foam therebycollapses in a middle of forming foam.

The curing time at the time when the above described foaming stocksolution is foamed and cured is preferably 10 minutes or shorter, and ismore preferably 7 minutes or shorter, in consideration of a productioncycle of a general flexible mold foam.

When the flexible mold foam is produced, each of the above describedcomponents can be mixed by using a high-pressure foaming machine, alow-pressure foaming machine or the like, similarly to the case of anordinary flexible mold foam.

It is preferable to mix the isocyanate component and the polyolcomponent just before forming foam. It is possible to premix the othercomponents with the isocyanate component or the polyol component withinsuch a range as not to affect the storage stability of the raw materialor the change over time in reactivity. Those mixtures may be usedimmediately after mixing, or after storage, a necessary amount may beused appropriately. In the case of a foaming apparatus into a mixingsection of which more than two components can be simultaneouslyintroduced, it is also possible to individually introduce the polyol,the foaming agent, the isocyanate, the catalyst, the foam stabilizer,the additive and the like, into the mixing section.

In addition, a mixing method may be any of dynamic mixing of performingmixing in mixing chamber in a machine head of a foaming machine, andstatic mixing of performing mixing in a liquid feeding pipe; or mayconcomitantly use both. There are many cases where mixing of a gaseouscomponent such as a physical foaming agent with a liquid component isperformed by the static mixing, and mixing of components that can bestably stored as a liquid is performed by dynamic mixing. It ispreferable that the foaming apparatus to be used in the presentinvention is a high pressure foaming apparatus which does not need towash the mixing section with a solvent.

The mixed solution obtained by such mixing is discharged into a metalmold (mold), is foamed and cured, and then is demolded. It is alsopreferable to previously apply a release agent to the metal mold, so asto smoothly perform the above described demolding. As for the releasingagent to be used, it is acceptable to use a releasing agent which isusually used in a molding and manufacturing field.

The demolded product can be used as it is, but it is preferable todestroy a cell membrane of the foam under compression or under reducedpressure by a conventionally known method, and to stabilize anappearance and dimension of a subsequent product.

By the method for producing the flexible polyurethane foam of thepresent invention, such a flexible polyurethane foam can be obtainedthat the apparent density is less than 40 kg/m³, the 25% compressionhardness of the foam test piece provided with the skin is 50 to 250N/314 cm², the coefficient of hysteresis loss is less than 30%, and thewet heat compression strain is less than 20%.

In addition, by the polyol component (A) containing the above describedcyclic glycol, the wet heat compression strain is further improved, andthe value can be controlled to less than 15%.

EXAMPLE

The present invention will be described more specifically in detailbased on Examples and Comparative Examples, but the present invention isnot limited to the following Examples. Incidentally, unless otherwisespecified, “parts” and “%” in the text are based on mass.

[Preparation of Polyol Composition]

Examples 1 to 10, and Comparative Examples 1 to 7

A reactor equipped with a stirrer, a cooling tube, a nitrogen inlet tubeand a thermometer was purged with nitrogen, and then 100 g of polyol 1,3 g of polyol 3, 1 g of a compatibilizing agent 1, 0.16 g of a catalyst1, 0.72 g of a catalyst 2, 1 g of a foam stabilizer 1 and 5.4 g of waterwere charged into the reactor; the mixture was stirred at 23° C. for 0.5hours; and a polyol composition (P-1) was obtained. Other polyolcompositions (P-2 to P-17) were also prepared similarly to P-1. Theresults are shown in Table 1 and Table 2.

TABLE 1 Example Example Example Example Example Example Example ExampleExample Example 1 2 3 4 5 6 7 8 9 10 Name of polyol P-1 P-2 P-3 P-4 P-5P-6 P-7 P-8 P-9 P-10 composition Polyol 1 100 100 100 100 100 100 100100 100 100 Polyol 2 Polyol 3 3 3 3 3 3 3 3 3 3 3 Glycol 1 8 4 Glycol 24 1.5 Compatibilizing agent 1 1 0.5 4.5 1 1 1 1 Compatibilizing agent 21 Compatibilizing agent 3 1 Compatibilizing agent 4 1 Compatibilizingagent 5 Compatibilizing agent 6 Compatibilizing agent 7 Compatibilizingagent 8 Compatibilizing agent 9 Catalyst 1 0.16 0.16 0.16 0.16 0.16 0.160.16 0.16 0.16 0.16 Catalyst 2 0.72 0.72 0.72 0.72 0.72 0.72 0.72 0.720.72 0.72 Foam stabilizer 1 1 1 1 1 1 1 1 1 1 Water 5.4 5.7 3.4 5.2 5.45.4 5.4 5.4 5.4 5.4 Storage stability of polyol ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯composition (25° C., 30 days)

TABLE 2 Comparative Comparative Comparative Comparative ComparativeComparative Comparative Example 1 Example 2 Example 3 Example 4 Example5 Example 6 Example 7 Name of polyol composition P-11 P-12 P-13 P-14P-15 P-16 P-17 Polyol 1 100 100 100 100 100 100 100 Polyol 2 15 Polyol 33 3 3 3 3 3 3 Glycol 1 Glycol 2 Compatibilizing agent 1 Compatibilizingagent 2 Compatibilizing agent 3 Compatibilizing agent 4 Compatibilizingagent 5 1 Compatibilizing agent 6 1 Compatibilizing agent 7 1Compatibilizing agent 8 1 Compatibilizing agent 9 1 Catalyst 1 0.16 0.160.16 0.16 0.16 0.16 0.16 Catalyst 2 0.72 0.72 0.72 0.72 0.72 0.72 0.72Foam stabilizer 1 1 1 1 1 1 1 Water 5.4 5.4 5.4 5.4 5.4 5.4 5.4 Storagestability of polyol X X X X X X X composition (25° C., 30 days)

Examples 11 to 20

A liquid temperature of a mixture (polyol composition) of all the rawmaterials except for a polyisocyanate compound among raw materials shownin Table 3 was adjusted to 24° C. to 26° C., and a polyisocyanatecomponent was adjusted at a liquid temperature of 24° C. to 26° C. Apredetermined amount of the polyisocyanate component was added to thepolyol composition, the mixture was mixed by a mixer (7000 revolutionsper minute) for 7 seconds, the mixed substance was injected into a mold,the flexible polyurethane foam was foamed, then the foam was taken outfrom the mold, and the obtained flexible polyurethane foam was subjectedto measurement of physical properties. For information, NCO Index inTable 3 is a ratio of NCO groups to the number of active hydrogen atomsexisting in the blend.

[Foaming Condition]

Mold temperature: 60 to 65° C.

Mold shape: 400 mm×400 mm×100 mm

Mold material: aluminum

Curing condition: 60 to 65° C.×5 minutes

TABLE 3 Example Example Example Example Example Example Example ExampleExample Example 11 12 13 14 15 16 17 18 19 20 P-1 100 P-2 100 P-3 100P-4 100 P-5 100 P-6 100 P-7 100 P-8 100 P-9 100 P-10 100 Isocyanate 172.0 72.2 71.8 71.9 72.0 72.0 77.7 74.9 71.1 71.6 NCO Index 85 85 85 8585 85 85 85 85 85 Apparent density 35 35 35 35 35 35 35 35 35 35 (kg/m³)25% ILD (N/314 110 108 111 109 110 109 114 113 113 111 cm²) Moldability◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ Coefficient of 28 27 28 28 27 28 28 27 27 28hysteresis loss (%) Wet heat 17 18 18 17 17 18 14 12 13 14 compressionstrain (%)

TABLE 4 Example Reference Reference Reference Reference Reference 11Example 1 Example 2 Example 3 Example 4 Example 5 P-1 100 100 100 100100 100 Isocyanate 1 72.0 Isocyanate 2 47.3 Isocyanate 3 72.0 Isocyanate4 72.0 Isocyanate 5 72.0 Isocyanate 6 72.0 NCO Index 85 85 85 85 85 85Density (kg/m³) 35 35 25% ILD (N/314 cm²) 110 80 Moldability ◯ ◯ X X X XCoefficient of hysteresis loss 28 26 (Shrinkage) (Collapse) (Collapse)(Shrinkage) (%) Wet heat compression strain 17 28 (%)

[Raw Materials Used]

-   -   Polyol 1: Polyoxyethylene polyoxypropylene polyol that is EL851        made by Asahi Glass Urethane Co., Ltd., in which an average        number of functional groups=3.0, and a hydroxyl value=24        (mgKOH/g).    -   Polyol 2: polyoxyethylene polyoxypropylene polyol that is        NEF-693 made by Tosoh Corporation, in which the average number        of functional groups=3.0, and the hydroxyl value=24 (mgKOH/g),        in which a primarization ratio of terminal ends=84%, and an        oxyethylene unit=14.6%.    -   Polyol 3: polyoxyethylene polyoxypropylene polyol that is        NEF-024 made by Tosoh Corporation, in which the average number        of functional groups=4.0, and the hydroxyl value=28 (mgKOH/g).    -   Glycol 1: CHDM-D (1,4-cyclohexanedimethanol, made by Eastman        Chemical Company), alicyclic glycol    -   Glycol 2: NEWPOL BPE-60 (polyoxyethylene bisphenol A ether, made        by Sanyo Chemical Industries, Ltd.), aromatic glycol    -   Compatibilizing agent 1: Demol NL (sodium salt of        β-naphthalenesulfonic acid formalin condensate, made by Kao        Corporation), anionic surfactant; aqueous solution of which a        solid content is 41%    -   Compatibilizing agent 2: Neoperex G-15 (sodium salt of        dodecylbenzenesulfonic acid, made by Kao Corporation), anionic        surfactant    -   Compatibilizing agent 3: Newcol N-291 PG (sodium salt of        di-2-ethylhexyl sulfosuccinate, made by Nippon Nyukazai Co.,        Ltd.), anionic surfactant    -   Compatibilizing agent 4: Perex TR (sodium salt of dialkyl        sulfosuccinate having 13 carbon atoms, made by Kao Corporation),        anionic surfactant    -   Compatibilizing agent 5: Newcol 1008 (polyoxyethylene        2-ethylhexyl ether, made by Nippon Nyukazai Co., Ltd.), alkyl        ether type surfactant    -   Compatibilizeing agent 6: Newcol 1305 (polyoxyethylene tridecyl        ether, made by Nippon Nyukazai Co., Ltd.), alkyl ether type        surfactant    -   Compatibilizing agent 7: PERSOFT EF-T (polyoxyethylene-alkyl        ether-sulfuric acid ester triethanol salt, made by NOF        Corporation), anionic surfactant    -   Compatibilizing agent 8: LATEMUL PD-104 (polyoxyalkylene alkenyl        ether ammonium sulfate, made by Kao Corporation), anionic        surfactant    -   Compatibilizing agent 9: Emulgen 102 KG (polyoxyethylene alkyl        ether, made by Kao Corporation), nonionic surfactant    -   Catalyst 1: 33% dipropylene glycol solution of        triethylenediamine, TEDA-L33 made by Tosoh Corporation    -   Catalyst 2: 1,2-dimethyl imidazole, TOYOCAT-DMI made by Tosoh        Corporation    -   Foam stabilizer: silicone-based foam stabilizer, Y-10366 made by        Momentive Corporation    -   Isocyanate 1: Polyphenylene polymethylene polyisocyanate of        which a rate of MDI content is 75 mass % and of which a rate of        isomer content is 38 mass % (CEF-536, made by Tosoh Corporation)    -   Isocyanate 2: toluene diisocyanate-based polyisocyanate        (CORONATE T-80, made by Tosoh Corporation)    -   Isocyanate 3: Polyphenylene polymethylene polyisocyanate of        which the rate of MDI content is 48 mass % and of which the rate        of isomer content is 18 mass % (CEF-531, made by Tosoh        Corporation)    -   Isocyanate 4: Polyphenylene polymethylene polyisocyanate of        which the rate of MDI content is 95 mass % and of which the rate        of isomer content is 18 mass % (CEF-532, made by Tosoh        Corporation)    -   Isocyanate 5: Polyphenylene polymethylene polyisocyanate of        which the rate of MDI content is 70 mass % and of which the rate        of isomer content is 5 mass % (CEF-533, made by Tosoh        Corporation)    -   Isocyanate 6: Polyphenylene polymethylene polyisocyanate of        which the rate of MDI content is 70 mass % and of which the rate        of isomer content is 60 mass % (CEF-534, made by Tosoh        Corporation)

[Evaluation of Moldability]

In the table, the evaluation of moldability “O” means that the flexiblepolyurethane foam can be molded without causing such a collapse that theurethane foam reaches a maximum height and then greatly sinks, or such aphenomenon that the formed urethane foam shrinks immediately afterhaving been foamed or after having been cured.

[Apparent Density]

An apparent density was determined according to the method described inJIS K 6400.

[25% Compression Hardness (25% ILD) of Foam Test Piece Provided withSkin]

The compression hardness was determined according to Method B describedin JIS K 6400.

[Coefficient of Hysteresis Loss]

The coefficient of hysteresis loss was measured according to Method Bdescribed in JIS K 6400.

[Wet Heat Compression Strain]

The compression strain was measured according to the method described inJIS K 6400.

[Stability Over Time of Polyol Composition]

A prepared polyol composition was charged into a sealed container of 200ml and was left at rest at 25° C. for 30 days, and then the presence orabsence of separation was visually checked.

As shown in Comparative Example 1 in Table 2, when the compatibilizingagent 1 is not used, compatibility cannot be sufficiently improved, andseparation results in occurring within 30 days. In addition, as shown inComparative Example 2, even though a polyether polyol has been usedwhich has a specific range of oxyethylene units and a specific amount ofa primarization ratio of terminal ends, the improvement of thecompatibility between the hydrophilic component and the hydrophobiccomponent in the polyol composition blended with a large amount of wateris insufficient, and the polyol composition results in being separatedwithin 30 days. In addition, as shown in Comparative Examples 3 to 7,even when a nonionic surfactant has been used as a compatibilizing agentand an anionic surfactant which does not have an alkali metal salt inthe hydrophilic portion have been used, the stability over times of thepolyol composition is poor, and the separation results in occurringwithin 30 days.

As shown in Examples 11 to 20 in Table 3, when flexible polyurethanefoams have been produced by use of the polyol compositions of Examples 1to 10, it is possible to obtain a molded body of which the apparentdensity is less than 40 kg/m³, of which the 25% compression hardness ofa foam test piece provided with a skin is 50 to 250 N/314 cm², of whichthe coefficient of hysteresis loss is less than 30%, and of which thewet heat compression strain is less than 20%.

Incidentally, as for the polyol compositions shown in ComparativeExamples 1 to 7, the flexible polyurethane foam is not produced, becausethe polyol compositions do not satisfy the stability over time.

In addition, as shown in Reference Example 1 of Table 4, it isunderstood that when the toluene diisocyanate-based polyisocyanate isused as the isocyanate component, there is the case where the value ofwet heat compression strain results in deteriorating. In addition, asshown in Reference Examples 2 to 5, it is understood that a flexiblepolyurethane foam having adequate moldability is not obtained, dependingon the rate of MDI content and the rate of isomer content of thepolyphenylene polymethylene polyisocyanate.

The flexible polyurethane foam obtained by the present invention isextremely useful for achieving both the performance and the weightreduction of a flexible foam for a seat cushion and a seat back forautomobiles.

According to the comparison between the above described examples andcomparative examples, in the present invention, it is possible to securethe compatibility between the hydrophobic component which is mainly thepolymer polyol and the hydrophilic component, and to thereby suppressseparation, even though a large amount of water has been mixed in thepolyol composition. In addition, it is clear that a molded body isobtained which has a low density and satisfies preferable physicalproperty values in the flexible polyurethane foam that uses the polyolcomposition, and it is possible to understand the significance andremarkable excellence of the constitution of the present invention.

Although the present invention has been described in detail and withreference to specific embodiments, it is apparent to those skilled inthe art that various changes and modifications can be made withoutdeparting from the essence and scope of the present invention.

The entire contents of the specifications, claims and abstracts ofJapanese Patent Application No. 2016-154423 filed on Aug. 5, in 2016,Japanese Patent Application No. 2016-208836 filed on October 25, in2016, Japanese Patent Application No. 2017-041994 filed on March 6, in2017 and Japanese Patent Application No. 2017-041995 filed on March 6,in 2017 are cited herein, and are incorporated as the disclosure of thespecification of the present invention.

1. A polyol composition for molding a flexible polyurethane foam,comprising: a polyol component (A); a catalyst (B); a foam stabilizer(C); a foaming agent (D); and a compatibilizing agent (E), wherein thecompatibilizing agent (E) is an anionic surfactant having a hydrophilicportion and a hydrophobic portion, and wherein the hydrophilic portionhas a salt consisting of an anionic polar group and an alkali metal, andthe hydrophobic portion has an aromatic ring, or alternatively thehydrophobic portion does not have an aromatic ring but contains 8 ormore carbon atoms in total.
 2. The polyol composition for molding aflexible polyurethane foam according to claim 1, wherein the alkalimetal salt of the hydrophilic portion of the compatibilizing agent (E)is a sodium salt.
 3. The polyol composition for molding a flexiblepolyurethane foam according to claim 1, wherein the compatibilizingagent (E) is an anionic surfactant having a sodium salt of anaphthalenesulfonic acid formalin condensate.
 4. The polyol compositionfor molding a flexible polyurethane foam according to claim 1, whereinthe compatibilizing agent (E) is an anionic surfactant having a sodiumsalt of a dialkyl sulfosuccinate.
 5. The polyol composition for moldinga flexible polyurethane foam according to claim 1, wherein thecompatibilizing agent (E) is an anionic surfactant having a sodium saltof an alkylbenzenesulfonic acid.
 6. The polyol composition for molding aflexible polyurethane foam according to claim 1, wherein thecompatibilizing agent (E) is contained in an amount of 0.1 to 5 mass %with respect to the polyol component (A).
 7. The polyol composition formolding a flexible polyurethane foam according to claim 1, wherein thepolyol component (A) comprises at least one cyclic glycol selected fromthe group consisting of alicyclic glycols and aromatic glycols.
 8. Thepolyol composition for molding a flexible polyurethane foam according toclaim 7, wherein a content of the at least one cyclic glycol selectedfrom the group consisting of alicyclic glycols and aromatic glycols is1.5 to 8 mass % with respect to the polyol component (A).
 9. A flexiblepolyurethane foam comprising: the polyol composition for molding aflexible polyurethane foam according to claim 1; and a polyisocyanatecomponent (F).
 10. The flexible polyurethane foam according to claim 9,wherein the polyisocyanate component (F) contains diphenylmethanediisocyanate in a range of 50 to 85 mass %, and a total amount of2,2′-diphenylmethane diisocyanate and 2,4′-diphenylmethane diisocyanatecontained in the diphenylmethane diisocyanate is 10 to 50 mass % withrespect to a total amount of the diphenylmethane diisocyanate.
 11. Theflexible polyurethane foam according to claim 9, wherein an apparentdensity is less than 40 kg/m³, and a 25% compression hardness of a foamtest piece provided with a skin is 50 to 250 N/314 cm².
 12. The flexiblepolyurethane foam according to claim 9, wherein a coefficient ofhysteresis loss is less than 30%, and a wet heat compression strain isless than 20%.
 13. A method for producing a flexible polyurethane foam,comprising reacting the polyol composition for molding a flexiblepolyurethane foam according to claim 1 with a polyisocyanate component(F).
 14. The method for producing a flexible polyurethane foam accordingto claim 13, wherein the polyisocyanate component (F) containsdiphenylmethane diisocyanate in a range of 50 to 85 mass %, and a totalamount of 2,2′-diphenylmethane diisocyanate and 2,4′-diphenylmethanediisocyanate contained in the diphenylmethane diisocyanate is 10 to 50mass % with respect to a total amount of the diphenylmethanediisocyanate.
 15. The method for producing a flexible polyurethane foamaccording to claim 13, wherein an apparent density of the flexiblepolyurethane foam to be obtained is less than 40 kg/m³, and a 25%compression hardness of a foam test piece provided with a skin is 50 to250 N/314 cm².
 16. The method for producing a flexible polyurethane foamaccording to claim 13, wherein a coefficient of hysteresis loss of theflexible polyurethane foam to be obtained is less than 30%, and a wetheat compression strain thereof is less than 20%.